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Peptide oostatic hormone → 1,3,5-Trimethoxy-2,4,6-trinitrobenzene

HRID 604971
ノート
印刷プレビュー

反応式

HRID 604971 の反応式
[CH3:1][C@H](NC([C@H]1N(C([C@@H](NC([C@@H](N)CC2C=CC(O)=CC=2)=O)CC(O)=O)=O)CCC1)=O)C(N1[C@H](C(N2[C@H](C(N3[C@H](C(N4[C@H](C(N5[C@H](C(N6[C@H](C(O)=O)CCC6)=O)CCC5)=O)CCC4)=O)CCC3)=O)CCC2)=O)CCC1)=O.COC1C([N+]([O-])=O)=C(O)C([N+]([O-])=O)=C(O)C=1[N+]([O-])=O.[CH3:95][O:96][C:97]1[C:105]([N+:106]([O-:108])=[O:107])=[C:104]([O:109][CH3:110])[C:103]([N+:111]([O-:113])=[O:112])=[C:102]([OH:114])[C:98]=1[N+:99]([O-:101])=[O:100]>>[CH3:95][O:96][C:97]1[C:105]([N+:106]([O-:108])=[O:107])=[C:104]([O:109][CH3:110])[C:103]([N+:111]([O-:113])=[O:112])=[C:102]([O:114][CH3:1])[C:98]=1[N+:99]([O-:101])=[O:100]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 5488810Peptide oostatic hormoneHCID 469097685-Methoxystyphnic acidHCID 469103023,5-Dimethoxypicric acid

生成物 1

HCID 113127111,3,5-Trimethoxy-2,4,6-trinitrobenzene

実験手順

Alkoxylating the nitrated alkoxy derivatives forms 1,3,5-trialkoxy-2,4,6-trinitrobenzene, which remains dissolved in the organic solvent to form a 1,3,5-trialkoxy-2,4,6-trinitrobenzene/organic solvent solution. Additional organic solvent may, optionally, be added to maintain an initial volume of the organic solvent in the reaction vessel such that the 1,3,5-trialkoxy-2,4,6-trinitrobenzene remains in solution. For example, the additional organic solvent may be added to the reaction vessel to maintain a volume of from about 10 mL to about 50 mL. In one embodiment, TMOF is used as the alkoxylating agent and is reacted with the 5-methoxystyphnic acid or 3,5-dimethoxypicric acid, producing 1,3,5-trimethoxy-2,4,6-trinitrobenzene. While the example described herein utilizes TMOF as the alkoxylating agent, triethyl orthoformate or tripropyl orthoformate may be used to form 1,3,5-triethoxy-2,4,6-trinitrobenzene or 1,3,5-tripropoxy-2,4,6-trinitrobenzene, respectively.

後処理

  1. additionAdditional organic solvent may, optionally, be added
  2. temperatureto maintain a volume of from about 10 mL to about 50 mL

出典と根拠

ORDレコード
ord-15d527ac3d51431382b3790729396a27
出典データセット
uspto-grants-2011_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07910776B2

反応ノート

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